Production of Multiprotein Complexes Using the Baculovirus Expression System: Homology-Based and Restriction-Free Cloning Strategies for Construct Design.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2021
Historique:
entrez: 10 12 2020
pubmed: 11 12 2020
medline: 1 4 2021
Statut: ppublish

Résumé

Most cellular processes are mediated by multi-subunit protein complexes which have attracted major interest in both academia and industry. Recombinant production of such entities in quantity and quality sufficient for functional and structural investigations may be extremely challenging and necessitate specific technologies. The baculovirus expression vector system is widely used for the production of eukaryotic multiprotein complexes, and a variety of strategies are available to assemble transfer vectors for the generation of recombinant baculoviruses. Here we detail applications of homology-based cloning techniques for one-step construction of dual promoter baculovirus transfer plasmids and of restriction-free (RF) cloning for the modification of existing constructs.

Identifiants

pubmed: 33301110
doi: 10.1007/978-1-0716-1126-5_2
doi:

Substances chimiques

Multiprotein Complexes 0
Recombinant Fusion Proteins 0
Recombinant Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-38

Références

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Auteurs

Paola Rossolillo (P)

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Centre National de la Recherche Scientifique (CNRS), UMR 7104, Institut National de la Santé et de la Recherche Médicale (INSERM), U1258, Université de Strasbourg, Illkirch, France. paola.rossolillo@igbmc.fr.

Olga Kolesnikova (O)

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Département of Integrated Structural Biology, Equipe Labellisée Ligue, Centre National de la Recherche Scientifique (CNRS), UMR 7104, Institut National de la Santé et de la Recherche Médicale (INSERM), U1258, Université de Strasbourg, Illkirch, France.
Structural and Computational Biology Unit, EMBL Heidelberg, Heidelberg, Germany.

Karim Essabri (K)

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Centre National de la Recherche Scientifique (CNRS), UMR 7104, Institut National de la Santé et de la Recherche Médicale (INSERM), U1258, Université de Strasbourg, Illkirch, France.

Gala Ramon Zamorano (GR)

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Département of Integrated Structural Biology, Equipe Labellisée Ligue, Centre National de la Recherche Scientifique (CNRS), UMR 7104, Institut National de la Santé et de la Recherche Médicale (INSERM), U1258, Université de Strasbourg, Illkirch, France.
Department of Life and Medical Sciences, University of Hertfordshire, Hatfield, UK.

Arnaud Poterszman (A)

Institut de Génétique et de Biologie Moléculaire et Cellulaire, Center for Integrated Biology, Integrated Structural Biology Department, Equipe labellisée Ligue Contre le Cancer, CNRS UMR 7104 - Inserm U 1258, University of Strasbourg, Illkirch, France. Arnaud.Poterszman@igbmc.fr.

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